Ann‐Kathrin Hauser

1.6k total citations · 1 hit paper
33 papers, 892 citations indexed

About

Ann‐Kathrin Hauser is a scholar working on Neurology, Physiology and Neurology. According to data from OpenAlex, Ann‐Kathrin Hauser has authored 33 papers receiving a total of 892 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Neurology, 15 papers in Physiology and 12 papers in Neurology. Recurrent topics in Ann‐Kathrin Hauser's work include Parkinson's Disease Mechanisms and Treatments (23 papers), Neurological diseases and metabolism (10 papers) and Lysosomal Storage Disorders Research (9 papers). Ann‐Kathrin Hauser is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (23 papers), Neurological diseases and metabolism (10 papers) and Lysosomal Storage Disorders Research (9 papers). Ann‐Kathrin Hauser collaborates with scholars based in Germany, Türkiye and Italy. Ann‐Kathrin Hauser's co-authors include Thomas Gasser, Claudia Schulte, Kathrin Brockmann, Daniela Berg, Walter Maetzler, Karin Srulijes, Stefanie Lerche, Isabel Wurster, Christian Deuschle and Milan Zimmermann and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and European Journal of Neuroscience.

In The Last Decade

Ann‐Kathrin Hauser

32 papers receiving 882 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

CSF α-synuclein seed amplification kinetic profiles are associated with cognitive decline in Parkinson’s disease

2024 34 citations Kathrin Brockmann, Stefanie Lerche et al. npj Parkinson s Disease profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ann‐Kathrin Hauser Germany	19	695	379	187	164	160	33	892
Konstantin Senkevich Russia	13	484 0.7×	345 0.9×	146 0.8×	198 1.2×	131 0.8×	51	761
Charles Duyckaerts France	6	672 1.0×	264 0.7×	274 1.5×	190 1.2×	214 1.3×	7	952
Florence Cormier‐Dequaire France	11	475 0.7×	171 0.5×	171 0.9×	136 0.8×	84 0.5×	13	675
Eleanna Kara United Kingdom	17	729 1.0×	352 0.9×	406 2.2×	322 2.0×	259 1.6×	25	1.1k
Anna Raunio Finland	10	653 0.9×	296 0.8×	233 1.2×	161 1.0×	155 1.0×	15	841
Stephanie A. Cobb United States	19	912 1.3×	311 0.8×	384 2.1×	312 1.9×	329 2.1×	27	1.2k
Mohamad Saad Egypt	5	477 0.7×	155 0.4×	212 1.1×	247 1.5×	216 1.4×	7	706
Hitoshi Takahashi Japan	9	467 0.7×	243 0.6×	342 1.8×	199 1.2×	179 1.1×	9	689
Neva West United States	6	557 0.8×	323 0.9×	276 1.5×	160 1.0×	106 0.7×	8	757
Ganqiang Liu China	12	321 0.5×	281 0.7×	67 0.4×	271 1.7×	85 0.5×	25	672

Countries citing papers authored by Ann‐Kathrin Hauser

Since Specialization

Citations

This map shows the geographic impact of Ann‐Kathrin Hauser's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ann‐Kathrin Hauser with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ann‐Kathrin Hauser more than expected).

Fields of papers citing papers by Ann‐Kathrin Hauser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ann‐Kathrin Hauser. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ann‐Kathrin Hauser. The network helps show where Ann‐Kathrin Hauser may publish in the future.

Co-authorship network of co-authors of Ann‐Kathrin Hauser

This figure shows the co-authorship network connecting the top 25 collaborators of Ann‐Kathrin Hauser. A scholar is included among the top collaborators of Ann‐Kathrin Hauser based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ann‐Kathrin Hauser. Ann‐Kathrin Hauser is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lerche, Stefanie, Isabel Wurster, Benjamin Röeben, et al.. (2025). Differences in age-related distribution of CSF alpha-synuclein seeding and Alzheimer profiles between PD with and without GBA1 variants. npj Parkinson s Disease. 11(1). 107–107.

Brockmann, Kathrin, Stefanie Lerche, Simone Baiardi, et al.. (2024). CSF α-synuclein seed amplification kinetic profiles are associated with cognitive decline in Parkinson’s disease. npj Parkinson s Disease. 10(1). 24–24. 34 indexed citations breakdown →

Simón‐Sánchez, Javier, Haşmet Hanağası, Başar Bılgıç, et al.. (2024). Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights. Journal of Medical Genetics. 61(5). 443–451. 6 indexed citations

Bılgıç, Başar, Betül Baykan, Erol Demir, et al.. (2022). Genotype–Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review. BMC Neurology. 22(1). 122–122. 6 indexed citations

Wurster, Isabel, Corinne Quadalti, Marcello Rossi, et al.. (2022). Linking the phenotype of SNCA Triplication with PET-MRI imaging pattern and alpha-synuclein CSF seeding. npj Parkinson s Disease. 8(1). 117–117. 9 indexed citations

Lerche, Stefanie, Simon Sjödin, Ann Brinkmalm, et al.. (2021). CSF Protein Level of Neurotransmitter Secretion, Synaptic Plasticity, and Autophagy in PD and DLB. Movement Disorders. 36(11). 2595–2604. 16 indexed citations

Brockmann, Kathrin, Corinne Quadalti, Stefanie Lerche, et al.. (2021). Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson’s disease and dementia with Lewy bodies. Acta Neuropathologica Communications. 9(1). 175–175. 72 indexed citations

Koros, Christos, Timo Strohäker, Claudia Schulte, et al.. (2021). A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease. Movement Disorders. 36(7). 1624–1633. 67 indexed citations

Lerche, Stefanie, Gerrit Machetanz, Isabel Wurster, et al.. (2019). Dementia with lewy bodies: GBA1 mutations are associated with cerebrospinal fluid alpha‐synuclein profile. Movement Disorders. 34(7). 1069–1073. 24 indexed citations

10.

Lerche, Stefanie, Isabel Wurster, Benjamin Röeben, et al.. (2019). Parkinson's Disease: Glucocerebrosidase 1 Mutation Severity Is Associated with CSF Alpha‐Synuclein Profiles. Movement Disorders. 35(3). 495–499. 38 indexed citations

11.

Schulte, Claudia, Mariana Moscovich, Florian G. Metzger, et al.. (2018). Cholinergic Pathway SNPs and Postural Control in 477 Older Adults. Frontiers in Aging Neuroscience. 10. 260–260. 3 indexed citations

12.

Keßler, Christoph, Haşmet Hanağası, Javier Simón‐Sánchez, et al.. (2017). Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey. Parkinsonism & Related Disorders. 48. 34–39. 9 indexed citations

13.

Hanağası, Haşmet, Anamika Giri, Ece Kartal, et al.. (2016). A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family. Parkinsonism & Related Disorders. 29. 117–120. 24 indexed citations

14.

Brockmann, Kathrin, Claudia Schulte, Christian Deuschle, et al.. (2015). Neurodegenerative CSF markers in genetic and sporadic PD: Classification and prediction in a longitudinal study. Parkinsonism & Related Disorders. 21(12). 1427–1434. 19 indexed citations

15.

Lohmann, Ebba, Ann‐Kathrin Hauser, Haşmet Hanağası, et al.. (2015). Clinical variability in ataxia–telangiectasia. Journal of Neurology. 262(7). 1724–1727. 21 indexed citations

16.

Giri, Anamika, Gamze Güven, Haşmet Hanağası, et al.. (2015). PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism. SHILAP Revista de lepidopterología. 6. 363–363. 14 indexed citations

17.

Pilotto, Andrea, Claudia Schulte, Ann‐Kathrin Hauser, et al.. (2015). GBA‐associated parkinsonism and dementia: beyond α‐synucleinopathies?. European Journal of Neurology. 23(3). 520–526. 7 indexed citations

18.

Brockmann, Kathrin, Karin Srulijes, Ann‐Kathrin Hauser, et al.. (2014). GBA ‐associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study. Movement Disorders. 30(3). 407–411. 191 indexed citations

19.

Weiß, Daniel, Sorin Breit, Ann‐Kathrin Hauser, et al.. (2012). Subthalamic nucleus stimulation restores the efferent cortical drive to muscle in parallel to functional motor improvement. European Journal of Neuroscience. 35(6). 896–908. 18 indexed citations

20.

Brockmann, Kathrin, Adriane Gröger, Adriana Di Santo, et al.. (2011). Clinical and brain imaging characteristics in leucine‐rich repeat kinase 2–associated PD and asymptomatic mutation carriers. Movement Disorders. 26(13). 2335–2342. 56 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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